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HE4, A New Potential Tumor Marker for Early Diagnosis and Predicting of Breast Cancer Progression
BACKGROUND & OBJECTIVE: This study examined the potential of human epididymis protein 4 (HE4) as a marker in early diagnosis or as a prognostic factor for breast cancer (BC) patients. METHODS: A total of 31 patients diagnosed with BC were enrolled in the study between 2008 and 2018. The mRNA and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iranian Society of Pathology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298057/ https://www.ncbi.nlm.nih.gov/pubmed/34306124 http://dx.doi.org/10.30699/IJP.2021.135323.2482 |
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author | Mirmohseni Namini, Nazanin Abdollahi, Alireza Movahedi, Monireh Emami Razavi, Amirnader Saghiri, Reza |
author_facet | Mirmohseni Namini, Nazanin Abdollahi, Alireza Movahedi, Monireh Emami Razavi, Amirnader Saghiri, Reza |
author_sort | Mirmohseni Namini, Nazanin |
collection | PubMed |
description | BACKGROUND & OBJECTIVE: This study examined the potential of human epididymis protein 4 (HE4) as a marker in early diagnosis or as a prognostic factor for breast cancer (BC) patients. METHODS: A total of 31 patients diagnosed with BC were enrolled in the study between 2008 and 2018. The mRNA and protein expression levels of HE4 were analyzed by immunohistochemistry (IHC) and real-time polymerase chain reaction (PCR) in the BC tissue and the non-tumoral adjacent tissue. Using ELISA technique, HE4 plasma levels were also measured in 43 BC patients compared to 43 healthy individuals. The correlation between HE4 expression and clinicopathological features was then investigated. RESULTS: An increase in HE4 expression was observed at mRNA and protein levels in the BC group compared to the control group (P<0.01, P<0.0001, respectively). In addition, the relative expression of HE4 mRNA in BC patients showed a significant correlation with the differentiation grade of cancer cells (P<0.001). Plasma levels of HE4 was also associated with grade (P<0.0001), stage, and tumor size in BC patients (for both P<0.01). Patients with metastatic BC (P<0.01), lymphatic invasion, and lymph node involvement (for both P<0.05) showed significantly higher plasma levels of HE4 expression than patients without metastasis. CONCLUSION: According to our findings, upregulation of HE4 may be related to invasive BC phenotype. Measuring plasma levels of HE4 could be useful as a screening test in early diagnosis of BC. |
format | Online Article Text |
id | pubmed-8298057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Iranian Society of Pathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-82980572021-07-23 HE4, A New Potential Tumor Marker for Early Diagnosis and Predicting of Breast Cancer Progression Mirmohseni Namini, Nazanin Abdollahi, Alireza Movahedi, Monireh Emami Razavi, Amirnader Saghiri, Reza Iran J Pathol Original Article BACKGROUND & OBJECTIVE: This study examined the potential of human epididymis protein 4 (HE4) as a marker in early diagnosis or as a prognostic factor for breast cancer (BC) patients. METHODS: A total of 31 patients diagnosed with BC were enrolled in the study between 2008 and 2018. The mRNA and protein expression levels of HE4 were analyzed by immunohistochemistry (IHC) and real-time polymerase chain reaction (PCR) in the BC tissue and the non-tumoral adjacent tissue. Using ELISA technique, HE4 plasma levels were also measured in 43 BC patients compared to 43 healthy individuals. The correlation between HE4 expression and clinicopathological features was then investigated. RESULTS: An increase in HE4 expression was observed at mRNA and protein levels in the BC group compared to the control group (P<0.01, P<0.0001, respectively). In addition, the relative expression of HE4 mRNA in BC patients showed a significant correlation with the differentiation grade of cancer cells (P<0.001). Plasma levels of HE4 was also associated with grade (P<0.0001), stage, and tumor size in BC patients (for both P<0.01). Patients with metastatic BC (P<0.01), lymphatic invasion, and lymph node involvement (for both P<0.05) showed significantly higher plasma levels of HE4 expression than patients without metastasis. CONCLUSION: According to our findings, upregulation of HE4 may be related to invasive BC phenotype. Measuring plasma levels of HE4 could be useful as a screening test in early diagnosis of BC. Iranian Society of Pathology 2021 2021-06-12 /pmc/articles/PMC8298057/ /pubmed/34306124 http://dx.doi.org/10.30699/IJP.2021.135323.2482 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Mirmohseni Namini, Nazanin Abdollahi, Alireza Movahedi, Monireh Emami Razavi, Amirnader Saghiri, Reza HE4, A New Potential Tumor Marker for Early Diagnosis and Predicting of Breast Cancer Progression |
title | HE4, A New Potential Tumor Marker for Early Diagnosis and Predicting of Breast Cancer Progression |
title_full | HE4, A New Potential Tumor Marker for Early Diagnosis and Predicting of Breast Cancer Progression |
title_fullStr | HE4, A New Potential Tumor Marker for Early Diagnosis and Predicting of Breast Cancer Progression |
title_full_unstemmed | HE4, A New Potential Tumor Marker for Early Diagnosis and Predicting of Breast Cancer Progression |
title_short | HE4, A New Potential Tumor Marker for Early Diagnosis and Predicting of Breast Cancer Progression |
title_sort | he4, a new potential tumor marker for early diagnosis and predicting of breast cancer progression |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298057/ https://www.ncbi.nlm.nih.gov/pubmed/34306124 http://dx.doi.org/10.30699/IJP.2021.135323.2482 |
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